Intellectual Property Paralegal Jobs in Japan

職務内容 Job DescriptionClinical Regulatory Writer (CReW) is responsible for the authoring of clinical-regulatory documents that communicate the evidence base of product knowledge in a credible consistent and compliant way.CReW leads the authoring of the clinical parts of documents such as CSP / MIC...

Job Descriptionジェネラルアンドスペシャルティメディスン/感染症ワクチン領域での募集です本ポジションは将来的にCRMClinical Research Managerを担う人材の候補募集となりますが採用時は弊社の治験オペレーションを担うAssociate Clinical Research ManageraCRMとしてのキャリアスタートとなりますご本人の経験適性に応...

About 3E:We are a mission-driven company dedicated to creating a safer and more sustainable world!3E provides award-winning regulatory expertise and cutting-edge technology that seamlessly integrates data and intelligence regarding chemicals regulations products and supply chains for over 5000 custo...

エアリキードグループは フランス パリを本社とし全世界78カ国に展開する産業と健康に技術とサービスで貢献するガス事業の世界的リーダーであり創業100年以上の歴史を持つガス事業のグローバルにおけるパイオニアです全世界64500人の従業員グループ全体売上は205億ユーロになります日本エアリキードは1907年に創業また日本...

職務の目的専門領域営業が取り扱う製品の専任MRとして医師薬剤師等の医療関係者に本製品の情報提供を行い適正使用並びに薬物療法の向上に貢献する主な業務内容専門領域営業が取り扱う製品はバイオ医薬品で複数の適応症を有しておりその適応症に応じて専任的にMR活動を行います気管支喘息既存治療によっても喘息症状をコント...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Strategy and Compliance  Develop and implement legal strategies aligned with business goals. Ensure compliance with all applicable Japan laws including corporate labour and other statutory regulations. Monitor changes in legislation from time to time and advise management board on necessary actions....

1. Job Objective:Responsible for regulatory activities related to postapproval CMC (Chemistry Manufacturing and Controls) change management for pharmaceutical products contributing to the maintenance of a stable and continuous product supply. 2. Job Roles and Responsibilities:Post approval CMC chang...

Die Fraunhofer-Allianz Energie () ist eine der größten Energieforschungsorganisationen unseren 20 Mitgliedsinstitutionen forschen über 2.000 Mitarbeitende in den Bereichen Erneuerbare Energien Energieeffizienztechnologien intelligente Energienetze Energiespeicher sowie Gebäude und Komponenten.Hier...

1. ObjectivesResponsible for clinical development of the assigned project in Japan under the supervision of the Japan Development Leader (JDL) who assumes responsibility for development of all projects in Japan in the respective therapeutic/disease area (TA/DA). Exercises proactive leadership in the...

JOB DESCRIPTION:MAIN PURPOSE OF THE ROLEIndividual contributor representing the most common entry point for this career stream.Works under direct supervision.MAIN RESPONSIBILITIES Identifies and validates molecular targets that play a key role in a particular disease process. Studies origin relati...

職務内容 / Job DescriptionAssociate Director Clinical Quality Management (ADCQM) leads the planning and implementation of all quality activities adapting to changes in the environment through relevant Clinical Quality Management System. ADCQM is individual contributor and skill expert which meets o...

職務内容 / Job DescriptionClinical Site Lead (CSL) is a field-based role within Site Management & Monitoring (SMM) at AstraZeneca K.K. dedicated to supporting clinical trials within Japan. The CSL will be assigned to dedicated disease area and proactively drive site performance enhance site engagem...

職務内容Description: The PS Epidemiologist (PSEPI) serves as a study lead for Post Authorization Regulatory Commitment Studies (PARCS) including post-marketing database study and use-result survey accelerating the generation of valuable real-world evidence. Leveraging extensive clinical research exp...

職務内容 / Job DescriptionClinical Scientist (CS) is a clinical project lead with strong experience in multidisciplinary aspects of drug development and is accountable/responsible for generating clinical development strategy designing clinical development options and delivering successful clinical...

Job DescriptionAs the independent second line assurance function for R&D our mission in Quality Assurance is to achieve enduring excellence in auditing quality management quality risk assessment and enhance the R&D quality mindset for the benefit of our patients.The job holder is responsible for one...

Role DescriptionThe Personal Assistant to the Head of R&D Japan is responsible for performing a wide range of high impact executive administrative and project-oriented activities in direct support of the Head of R&D Japan and the R&D Japan leadership team. The role involves initiating and managing e...

職務内容 職務内容 / Job Description呼吸器領域の医療施設医師薬剤師に対する医薬品の情報提供活動および適正使用の推進 応募資格(経験資格等) / Qualification (Experience & Skill etc.)Typical AccountabilitiesEducation Qualifications Skills and Experiencee必須 / Mandatory

職務概要臨床試験のデザイン分析解釈を関連する薬事規制要件標準業務手順書SOPおよびベストプラクティスに従って業務を行う臨床開発チームの中で特に臨床開発リーダー臨床薬理担当者統計担当者で効果的に協働し科学に基づいた統計の専門知識を生かし医薬品開発に貢献する職務内容試験デザイン統計解析計画統計解析結果の解...

Job Description業務内容1. グローバル戦略に沿った効率的かつ付加価値の高い新薬等の国内開発薬事戦略の構築2. 規制当局厚生労働省独立行政法人医薬品医療機器 総合機構などとの窓口業務3. 承認申請審査資料機構相談資料照会事項に対する回答等へのレビューアドバイスを通じ当局提出文書の質の向上に資する4. 承認申請審査...